Canonical Allele Identifier: CA2660747013
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112831128-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831128G>T , CM000664.2:g.112831128G>T GRCh38
NC_000002.11:g.113588705G>T , CM000664.1:g.113588705G>T GRCh37
NC_000002.10:g.113305176G>T NCBI36
NG_008851.1:g.10652C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+164C>A MANE Select ENSP00000263341.2:n.597+164C>A
ENST00000263341.6:c.597+164C>A ENSP00000263341.2:n.597+164C>A
ENST00000491056.5:n.1404+164C>A
NM_000576.2:c.597+164C>A NP_000567.1:n.597+164C>A
XM_006712496.1:c.363+164C>A XP_006712559.1:n.363+164C>A
XM_017003988.2:c.504+164C>A XP_016859477.1:n.504+164C>A
NM_000576.3:c.597+164C>A MANE Select NP_000567.1:n.597+164C>A
Search 100 bp 5'
Search 100 bp 3'